Search

Here, a tetrakaidecahedron-shaped Cu four-core supramolecule was designed to overcome the defects of supramolecules for lithium-ion batteries. With multiple metal centers, conductive ligands and abundant hydrogen bonds, this novel electrode shows excellent rate capability (459.4 mA h g

Severe particle aggregation and performance fading hinder the application of Mn-based chalcogenides (MBCs) in sodium-ion batteries, and most modifications focus on complicated structure design. Wit...

The persulfate-based advanced oxidation process has been an effective method for refractory organic pollutants’ degradation in aqueous phase. Herein, α-MnO2 with nanowire morphology was facially fabricated via a one-step hydrothermal method and successfully activated peroxymonosulfate (PMS) for Rhodamine B (RhB) degradation. Influencing factors, including the hydrothermal parameter, PMS concentration, α-MnO2 dosage, RhB concentration, initial pH, and anions, were systematically investigated. The corresponding reaction kinetics were further fitted by the pseudo-first-order kinetic. The RhB degradation mechanism via α-MnO2 activating PMS was proposed according to a series of quenching experiments and the UV-vis scanning spectrum. Results showed that α-MnO2 could effectively activate PMS to degrade RhB and has good repeatability. The catalytic RhB degradation reaction was accelerated by increasing the catalyst dosage and the PMS concentration. The effective RhB degradation performance can be attributed to the high content of surface hydroxyl groups and the greater reducibility of α-MnO2, and the contribution of different ROS (reactive oxygen species) was 1O2 > O2·− > SO4·− > ·OH.

With advantages of high theoretical capacity and low cost, manganese sulfide (MnS) has become a potential electrode material for sodium-ion batteries (SIBs). However, complicated preparations and limited cycle life still hinder its application. Inspired by cream rolls in our daily life, a MnS/N,S-co-doped carbon tube (MnS/NSCT) composite with a 3D cross-linked tubular structure is prepared via an ultra-simple and low-cost method in this work. As the anode for SIBs, the cream roll-like MnS/NSCT composite has delivered the best electrochemical performance to date (the highest capacity of 550.6 mA h g−1 at 100 mA g−1, the highest capacity of 447.0 mA h g−1 after 1400 cycles at 1000 mA g−1, and the best rate performance of 319.8 mA h g−1 at 10 000 mA g−1). Besides, according to several in situ and ex situ techniques, the sodium storage mechanism of MnS/NSCTs is mainly from a conversion reaction, and the superior electrochemical performance of MnS/NSCTs is mainly attributed to the unique cream roll-like structure. More importantly, this simple method may be feasible for other anode materials, which will greatly promote the development of SIBs.

In recent years, the sodium storage mechanism and performance optimization of FeS2 have been studied intensively. However, before the commercial application of FeS2, preconditions of low-cost, simple craft and scale production of nanoscale FeS2 are also essential. Based on above challenges, mesh-like FeS2/carbon tube/FeS2 composites are prepared simply from green, low-cost and renewable natural herb in this work. With the assistance of protogenetic interconnected carbon tube network (only 5.3 wt%), FeS2/carbon tube/FeS2 composites show high capacity (542.2 mA h g−1), good stability (< 0.005% per cycle over 1000 cycles), and excellent rate performance (426.2 mA h g−1 at 2 A g−1). The outstanding electrochemical performance of FeS2/carbon tube/FeS2 composites may be attributed to the unique interconnected reticular structure, meaning that FeS2 nanoparticles are effectively immobilized by carbon tube network via physical encapsulation and chemical bonding. More importantly, this work may provide green and low cost preparation method for specially structured metal sulfides/carbon composites, which promotes their commercial utilization in environmentally friendly energy storage system. Keywords: FeS2, Biomass-drived carbon, Mesh-like structure, Low cost, Sodium-ion batteries

CdS has attracted extensive attention in the photocatalytic degradation of wastewater due to its relatively narrow bandgap and various microstructures. Previous reports have focused on CdS coupled with other semiconductors to reduce the photocorrosion and improve the photocatalytic performance. Herein, a 3D hierarchical CdS/Cu7S4 nanostructure was synthesized by cation exchange using lily-like CdS as template. The heterojunction material completely inherits the special skeleton of the template material and optimizes the nano-scale morphology, and achieves the transformation from nanometer structure to quantum dots (QDs). The introduction of Cu ions not only tuned the band gap of the composites to promote the utilization of solar photons, more importantly, Fenton-like catalysis was combined into the degradation process. Compared with the experiments of organic dye degradation under different illumination conditions, the degradability of the CdS/Cu7S4 QDs is greatly superior to pure CdS. Therefore, the constructed CdS/Cu7S4 QDs further realized the optimization of degradation performance by the synergic effect of photo-catalysis and Fenton-like catalysis.

The lithiation induced stress in multilayer silicon/graphite-based electrodes for lithium ion batteries is evaluated analytically. Firstly, the silicon/graphite-based composite active layer is reinforced by Ti3C2 MXene, and the effects of Ti3C2 MXene additive on elastic modulus of the active layer are discussed based on the Halpin–Tsai empirical equation. Secondly, biaxial stresses in both bilayer and symmetric trilayer silicon/graphite-based electrodes are estimated by a mechano-electrochemical model, which is derived by imitating thermal expansion stress in layered structural components. And the effects of Ti3C2 MXene’s parameters, including additive amount, number of layers and length–width ratio, on the stress in multilayer silicon/graphite-based electrodes are also be discussed in detail. Finally, based on the numerical analysis, some design strategies for Ti3C2 MXene reinforced composite active layer are proposed from mechanical views.

A new synergetic anticorrosion system was constructed via combining a self-powered cathodic protection based on triboelectric nanogenerator (TENG) and a green corrosion inhibitor of zinc gluconate (ZnG). Wind-driven TENG with a sandwich-like structure was designed, exhibiting high output performance with the peak values of short circuit current, output voltage and corresponding power reaching about 155 μA, 402 V and 13.5 mW, respectively, under a wind speed of 10 m/s. With the assistance of TENG, the migration of corrosion inhibitor can be accelerated and the formation of the protective layer becomes faster due to the driving force of electric field. The shielding effect of protective layer in turn improves the cathodic protection of TENG. The immersion experiment and electrochemical measurements including Tafel polarization curves and EIS were taken to evaluate the performance of synergetic anticorrosion system. FESEM and EDS measurements were performed to analyze the morphology and composition of the protective layer and confirm the mechanism of synergetic anticorrosion. This work expands the application of TENG in the anticorrosion field and proposes a new thought of synergetic anticorrosion method.

Heterostructures show excellent performance in energy and environment fields due to the unique interface structure and synergistic effect of multi-components. Here, we introduce a stepwise method to prepare multi-element Co3O4@C@MnO2 heterostructures on nickel foam as binder-free supercapacitor electrode material, where crystalline Co3O4 acts as intimal “core” and wrinkled ultrathin MnO2 nanosheets as the outer “shell”. In three-electrode mode, Co3O4@C@MnO2 shows excellent electrochemical performance with a high cyclic specific capacitance of 1335.3 F g−1 at a current density of 20 A g−1. Furthermore, the asymmetry supercapacitor device assembled with Co3O4@C@MnO2 heterostructures and active carbon exhibits high specific capacity (126.6 F g−1 at a current density of 0.5 A g−1) and long life (about 61 F g−1 at a relatively high current of 20 A g−1 after 40,000 cycles). Compared with Co3O4@MnO2 or C@MnO2, the improved performance of Co3O4@C@MnO2 heterostructures is proposed to be attributed to the synergistic effect in multi-components. Remarkably, the introduction of C between Co3O4 and MnO2 could promote the electron transfer, reduce the impedance and thus improve the electrochemical performance of the heterostructures.

We demonstrate the availability of Fe 7 Se 8 as anode for sodium-ion batteries (SIBs) for the first time. A Fe 7 Se 8 nanocomposite encapsulated by nitrogen-doped carbon layers (Fe 7 Se 8 @NC) has been fabricated via a facile thermal method using Prussian Blue as precursor, and its sodium storage mechanisms and extraordinary activation process during cycling are revealed for comprehensive understanding of its reaction process. It shows that the sodium storage mechanisms of Fe 7 Se 8 can be affected by the activation process, especially in the charge process. As SIB anode material, the Fe 7 Se 8 @NC exhibits an outstanding electrochemical performance with a reversible discharge capacity of 367 mAh g −1 at 500 mA g −1 . Even at 2000 mA g −1 , the capacity can retain 251 mAh g −1 . Moreover, the Fe 7 Se 8 @NC shows excellent cyclability, which maintains the capacity up to 339 mAh g −1 at 1000 mA g −1 after 1200 cycles. The results demonstrate that Fe 7 Se 8 @NC is a promising anode material for SIBs.

Pyrite FeS2 has attracted extensive interest as anode material for sodium-ion batteries due to its high capacity, low cost, and abundant resource. However, the micron-sized FeS2 usually suffers from poor cyclability, which stems from structure collapse, exfoliation of active materials, and sulfur dissolution. Here, we use a synergistic approach to enhance the sodium storage performance of the micron-sized FeS2 through voltage control (0.5–3 V), binder choice, and graphene coating. The FeS2 electrode with the synergistic approach exhibits high specific capacity (524 mA h g–1), long cycle life (87.8% capacity retention after 800 cycles), and excellent rate capability (323 mA h g–1 at 5 A g–1). The results prove that a synergistic approach can be applied in the micron-sized sulfides to achieve high electrochemical performance.

Sodium iron hexacyanoferrate (Fe-HCF) is regarded as a potential cathode material for sodium-ion batteries (SIBs) due to its high specific capacity, low cost, facile synthesis and environmentally friendly. However, Fe-HCF always suffers from poor electronic conductivity, low crystallinity and side reactions with electrolyte, leading to poor rate performance, low coulombic efficiency and deterioration of cycling stability. Herein, we report a green and facile synthesis to encapsulate Fe-HCF microcubes with potassium nickel hexacyanoferrate (Ni-HCF). The core-shell Fe-HCF@Ni-HCF composite delivers a reversible capacity of 79.7 mAh g−1 at 200 mA g−1 after 800 cycles and a high coulombic efficiency of 99.3%. In addition, Fe-HCF@Ni-HCF exhibits excellent rate performance, retaining 60 mAh g−1 at 2000 mA g−1. The results show that Fe-HCF@Ni-HCF integrates the advantages of both Fe-HCF and Ni-HCF, making it electrochemically stable as cathode material for SIBs.

Gamma titanium phosphate (G-TiP) possesses a lamellar framework with larger interlayer spacing than α-type TiP, in which the protons within the P–OH groups can be exchanged by alien ions. Herein, the electrochemical performance of the bulk G-TiP in both lithium and sodium storage has been systematically investigated. The results reveal that the layered G-TiP can store both Li+ and Na+ ions via a local ion exchange process and redox reaction in a wide voltage range. Despite the large radius of Na+, G-TiP exhibits a higher structural tolerance upon (de)sodiation and better capacity retention when cycled at low voltage. For a Na-ion cell, the G-TiP electrode delivers a specific capacity of 161.3 mA h g−1 within 0.1–2.8 V, showing an obvious plateau in the range of 1.6–2.2 V with a solid solution reaction. For a Li-ion cell, a reversible capacity of 109 mA h g−1 is attained within 0.8–2.8 V, and a voltage plateau occurs at 2.2–2.6 V.

Exploring simple synthesis method of high-performance sodium-ion batteries (SIBs) electrode materials has always been highly concerned in large-scale energy storage technology filed. Here, ultrathin two-dimensional (2D) FexCo1-xSe2 nanosheets as anode material for SIBs are successfully synthesized by one-step solvothermal method. The average thickness of Fe0·08Co0·92Se2 nanosheets is approximately 3.08 nm, which is about equivalent to the thickness of six b-axis crystal cells. When employed as anode for SIBs, Fe0·08Co0·92Se2 nanosheets display a high initial discharge specific capacity of 679.8 mAh/g, a high initial coulombic efficiency of 85.5% and superior reversible specific capacity of 510.4 mAh/g at 1 A/g. Simultaneously, Fe0·08Co0·92Se2 also exhibits an enhanced rate capability (480.0, 460.0, 435.1 mAh/g at 0.2, 2, 4 A/g respectively) and outstanding cycling stability at relatively large current density (397.0 mAh/g at 4 A/g after 1000 cycles). The excellent Na-ion storage performance of FexCo1-xSe2 nanosheets could be ascribed to the abundant electrochemical active sites and shorten ion transfer tunnels provided by this ultrathin 2D structure and bimetallic ion synergistic effect by heteroatom doping. Noticeably, the capacitive contribution may play the key role in the admirable rate capability through electrochemical kinetics analysis of Fe0·08Co0·92Se2 nanosheets. Therefore, this work presents a simple preparation of ultrathin 2D selenide nanosheets and an effective low-cost regulation strategy for improving Na-ion storage performance.

CdS has attracted extensive attention in the photocatalytic degradation of wastewater due to its relatively narrow bandgap and various microstructures. Previous reports have focused on CdS coupled with other semiconductors to reduce the photocorrosion and improve the photocatalytic performance. Herein, a 3D hierarchical CdS/Cu

Carbon coated K0.8Ti1.73Li0.27O4 (KTLO) has been synthesized by a facile flux method followed by ball-milling and gaseous carbon coating. The carbon coated KTLO delivers a reversible specific capacity of 119.6 mA h g(-1) at 20 mA g(-1) with no capacity loss after 250 cycles as an anode material in sodium ion batteries, exhibiting an improved rate capability of 66 mA h g(-1) at 200 mA g(-1). It was found that carbon coating of KTLO not only enhances its electronic conductivity, but also improves the structure stability, proving that the carbon coated KTLO is a promising anode material for sodium ion batteries.

Nanostructured δ-MnO2 incorporated with alkali cations (A-δ-MnO2, A = K+, Na+) has been synthesized and evaluated as a cathode material for aqueous sodium-ion batteries. It is observed that Na+ ions are easier than K+ ions to intercalate into the layered δ-MnO2 due to their smaller ion radius. The incorporation of K+ and Na+ into δ-MnO2 shows a great influence on the electrochemical performance of the layered δ-MnO2. The full cell with (K, Na)-co-incorporated δ-MnO2 (K : Na : Mn = 0.15 : 0.26 : 1) hierarchical nanospheres as the cathode and NaTi2(PO4)3 as the anode exhibits a specific capacity of 74.6 mA h g−1 at 150 mA g−1, and the capacity remains at ∼62% at a high current density of 600 mA g−1. The electrochemical cycling does not induce observable structural degradation even after 200 cycles. K-incorporated and (K, Na)-co-incorporated δ-MnO2 electrodes have superior capacity and rate capability, which can be ascribed to their hierarchical structure and adequate crystallinity.

Although sodium-ion batteries (SIBs) are considered as alternatives to lithium-ion batteries (LIBs), the electrochemical performances, in particular the energy density, are much lower than LIBs. A metal–organic compound, cuprous 7,7,8,8-tetracyanoquinodimethane (CuTCNQ), is presented as a new kind of cathode material for SIBs. It consists of both cationic (CuII↔CuI) and anionic (TCNQ0↔TCNQ−↔ TCNQ2−) reversible redox reactions, delivering a discharge capacity as high as 255 mAh g−1 at a current density of 20 mA g−1. The synergistic effect of both redox-active metal cations and organic anions brings an electrochemical transfer of multiple electrons. The transformation of cupric ions to cuprous ions occurs at near 3.80 V vs. Na+/Na, while the full reduction of TCNQ0 to TCNQ− happens at 3.00–3.30 V. The remarkably high voltage is attributed to the strong inductive effect of the four cyano groups.

Pyrite FeS

Metal sulfides have attracted much attention as anode for sodium-ion batteries (SIBs) due to their high specific capacity and low price. Among all the sulfides, MnS has shown a high theory capacity of 610 mAh g-1 in SIBs1. However, the sodium storage performance of MnS was rather poor because of its poor conductivity and drastic volume changes during their conversion reaction process. In order to solve this problem, it’s essential to design the MnS material with both electron transportation pathway and solid supporting matrix. Herein, a MnS/porous carbon fibers (MnS/PCFs) composite was synthesized by the electrospun method. The MnS/PCFs composite has several advantages. Firstly, MnS nanoparitcles were embedded in porous carbon fibers, which can suppress the volume change and materials exfoliation. Secondly, abundant interconnected pores facilitate the electrolyte infiltration and ion transport. Furthermore, 1D nanofibers can form a 3D interconnected conductive network and reduce the resistance. Remarkably, the MnS/PCFs composite exhibits high specific capacity (523.6 mAh g-1), long cycling life (78.4% for 760 cycles) and excellent rate capability (301.4 mAh g-1 at 2 A g-1). MnS/PCFs with different carbon contents were synthesized via a simple electrospinning method. Firstly, manganese acetate, polyacrylonitrile and polymethyl methacrylate were mixed in DMF and electrospuned. Then the as-spun fibers were carbonized and vulcanized to obtain the MnS/PCFs composites. The sodium performance of MnS/PCFs with different carbon content is systematically investigated, and the MnS/PCFs-0.8 sample (31.3 wt% carbon) exhibits the best cycling and rate properties, delivering a specific capacity of 523.6 mA h g-1 at 100 mA g-1. After 700 cycles, the capacity still remains 78.4%. At a high current of 2 A g-1, MnS/PCFs-0.8 exhibit the highest capacity of 301.4 mA h g-1. The SEM and TEM images of MnS/PCFs-0.8 proved the uniform distribution of MnS nanoparticles in porous carbon. The CV curves of MnS/PCFs are shown in Figure 1e. The reduction peaks at 1.2 V may assign to the Na+ insertion into the MnS, and the peaks at 0.6 V corresponds to the conversion reactions to form Na2S and Mn. The oxidation peak at 0.9 V is attributed to the conversion reaction of Na2S and Mn, and the peaks as 1.7 V and 1.95 V indicate a multistep extraction process of Na+from MnS. Detailed electrochemical process are also detected by other test. In conclusion, MnS/PCFs were prepared by an electrospinning method. The hollow nanofiber structure could not only suppress the volume change of MnS, but also facilitate electrolyte infiltration and ion transport. Furthermore, 3D interconnected conductive network will reduce the resistance and enhance the rate capability of MnS. Remarkably, the MnS/PCFs composite with proper carbon content exhibits high specific capacity (523.6 mAh g-1), long cycle life (78.4% for 760 cycles) and excellent rate capability (301.4 mAh g-1 at 2 A g-1). References 1 Y. Liu, Y. Qiao, W. X. Zhang, Z. Li, X. L. Hu, L. X. Yuan and Y. H. Huang, J. Mater. Chem., 2012, 22, 24026-24033. 2 X. J. Xu, S. M. Ji, M. Z. Gu and J. Liu, ACS Appl. Mat. Interfaces, 2015, 7, 20957-20964. Figure 1